rs864622273

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs864622273(A;A)

Make rs864622273(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

62813412

Gene

EGR2

is a	snp
is	mentioned by
dbSNP	rs864622273
dbSNP (classic)	rs864622273
ClinGen	rs864622273
ebi	rs864622273
HLI	rs864622273
Exac	rs864622273
Gnomad	rs864622273
Varsome	rs864622273
LitVar	rs864622273
Map	rs864622273
PheGenI	rs864622273
Biobank	rs864622273
1000 genomes	rs864622273
hgdp	rs864622273
ensembl	rs864622273
geneview	rs864622273
scholar	rs864622273
google	rs864622273
pharmgkb	rs864622273
gwascentral	rs864622273
openSNP	rs864622273
23andMe	rs864622273
SNPshot	rs864622273
SNPdbe	rs864622273
MSV3d	rs864622273
GWAS Ctlg	rs864622273

Max Magnitude

0

ClinVar
Risk	rs864622273(A;A)
Alt	rs864622273(A;A)
Reference	Rs864622273(G;G)
Significance	Pathogenic
Disease	Charcot-Marie-Tooth disease not provided
Variation	info
Gene	EGR2
CLNDBN	Charcot-Marie-Tooth disease, type I not provided
Reversed	1
HGVS	NC_000010.10:g.64573172C>T
CLNSRC
CLNACC	RCV000206846.1, RCV000431412.1,